部分構造検索

CCCCCCNCc1ccccc1

Cc1cccc(C)c1C(=O)NC(c1cccc(N2CCOCC2)c1)C12CCC(CC1)N2C
Reaction #738
収率 18.0%
CCCN(CCC)[C@H]1Cc2c(C(C)=O)ccc3c2[C@@H](CN3)C1
Reaction #5521
oil
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)[C@@H]1Cc2c(Br)ccc3c2[C@H](CN3)C1
Reaction #83619
(-)(2aR,4S)-6-bromo-4-(di-n-propylamino)-1,2,2a,3,4,5-hexahydrobenz[cd]indole
収率 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)[C@@H]1Cc2c(C=O)ccc3c2[C@@H](C1)CN3C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #83620
above-titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)[C@H]1Cc2c(I)ccc3c2[C@@H](CN3)C1
Reaction #83630
debenzoylated product
収率 96.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cc(N3CCN(CCCCC4(C(=O)O)c5ccccc5-c5ccccc54)CC3)ccc2CN1C1CCCCC1
Reaction #175064
DOI: 10.1039/C8SC04228D
CC1CN(c2ccc3c(Cl)cccc3n2)CC(C)N1CCCCC1(C(=O)NCc2ccc(F)cc2)c2ccccc2-c2ccccc21
Reaction #181428
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc2c(c1)CC1C2CCCN1C(=O)c1ccc2[nH]cnc2c1
Reaction #184985
DOI: 10.1039/C8SC04228D
CC1CN(c2nc3ccccc3s2)CC(C)N1CCCCC1(C(=O)NCc2ccc(F)cc2)c2ccccc2-c2ccccc21
Reaction #194408
DOI: 10.1039/C8SC04228D
CCCC1CCC(NCc2cc3c(cc2OC)C2CC2C(=O)N3C)C(c2ccccc2)N1
Reaction #197699
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(F)cc1)C1(CCCCN2CCN(c3nc4ccccc4s3)CC2)c2ccccc2-c2ccccc21
Reaction #203007
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(F)cc1)C1(CCCCN2CCN(c3ccc4cccc(Cl)c4n3)CC2)c2ccccc2-c2ccccc21
Reaction #204432
DOI: 10.1039/C8SC04228D
O=C(c1cccc(N2CCN(CCCCC3(C(=O)NCC(F)(F)F)c4ccccc4-c4ccccc43)CC2)c1)N(Cc1ccccc1)C1CCCCC1
Reaction #204621
DOI: 10.1039/C8SC04228D
CC(C)(C)C1CCC(NCc2ccc(C(=O)N(CCC(=O)O)CC3CC3)cc2)CC1
Reaction #207835
DOI: 10.1039/C8SC04228D
CCCN(CCC)[C@@H]1Cc2c(Br)ccc3c2[C@@H](C1)CN3C(=O)c1ccccc1
Reaction #216960
desired product
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Br
Reaction #224005
DOI: 10.1039/C8SC04228D
CC1CN(c2ccc3ccccc3n2)CC(C)N1CCCCC1(C(=O)NCc2ccc(F)cc2)c2ccccc2-c2ccccc21
Reaction #228122
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)N2CCC(C(=O)C3CCCCC3)CC2)c([N+](=O)[O-])cc1OC
Reaction #230818
DOI: 10.1039/C8SC04228D
COc1ccc(COC(c2ccccc2)(c2ccc(OC)cc2)C2CN(C(=O)CCCCCN3C(=O)c4ccccc4C3=O)CC2OC(=O)CCC(=O)O)cc1
Reaction #230950
DOI: 10.1039/C8SC04228D
CCCN(CCC)C1Cc2c(C=O)ccc3c2C(C1)CN3C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #233350
DOI: 10.1039/C8SC04228D
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