반응 #9858

ord-812a26b6b0914c49893210dc67586be6

반응 방정식

OC(c1cc2cnc(NC3CCOCC3)nc2s1)c1ccccc1F
alcohol
OC(c1cc2cnc(NC3CCOCC3)nc2s1)c1ccccc1F
2-(tetrahydropyran-4-ylamino)-6-[(2-fluorophenyl)hydroxylmethyl]thieno[2,3-d]pyrimidine
CC[SiH](CC)CC
triethylsilane
O=C(O)C(F)(F)F
trifluoroacetic acid
Fc1ccccc1Cc1cc2cnc(NC3CCOCC3)nc2s1
final product
Fc1ccccc1Cc1cc2cnc(NC3CCOCC3)nc2s1
2-(tetrahydropyran-4-ylamino)-6-[(2-fluorophenyl)methyl]thieno[2,3-d]pyrimidine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvents were removed
  2. 2
    workup.ADDITIONThe residue was diluted with toluene (5 mL)
  3. 3
    농축concentrated
  4. 4
    기타Purification with preparative TLC (50% EtOAc/Hexanes)

실험 절차

The alcohol (140 mg) obtained in Example 2A was stirred with triethylsilane (1.0 mL) and trifluoroacetic acid (1.5 mL) in dichloromethane (5 mL) for 4 hours. The solvents were removed. The residue was diluted with toluene (5 mL) and then concentrated. This dilution-concentration process was repeated three times. Purification with preparative TLC (50% EtOAc/Hexanes) gave the final product. It was converted to the hydrochloride salt with 1N HCl in ether to yield 65 mg of the salt. MP: 217–219° C. MS: 344 (M+H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091347B2uspto-grants-2006_08