Phenyl Isothiocyanate → HCID 86640127, compound

Participants

Reaction Steps

Using bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine (80.0 mg, 0.148 mmol) and phenyl isothiocyanate (53.0 μl, 0.447 mmol) instead of o-tolyl isothiocyanate, thiourea was formed in the same manner as Example 1-D-210, to obtain a crude product of 4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidine-7-carbothioic acid phenylamide as a brown solid (155 mg), and then the PMB groups were removed according to the above Deprotection method 3, to obtain the desired compound (D-216) as a yellow powder (34.5 mg, 55%).

Provenance & Evidence